HIGH

Wizcure Pharmaa Recalls Ophthalmic Strips Over Sterility Concerns

Wizcure Pharmaa recalled 50,400 boxes of Bio Glo Fluorescein Sodium Ophthalmic Strips on December 31, 2025. The recall follows concerns regarding lack of assurance of sterility, as products did not conform to good manufacturing practices. Consumers should stop using the product immediately and consult healthcare providers.

Quick Facts at a Glance

Recall Date
December 31, 2025
Hazard Level
HIGH
Brand
Wizcure Pharmaa
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Wizcure Pharmaa Private Limited or your healthcare provider for guidance. Notification method: Letter

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Product Details

The recall affects Bio Glo Fluorescein Sodium Ophthalmic Strips USP, with 300 diagnostic strips per box. The product was manufactured by Omni Lens Pvt Ltd in Ahmedabad, India, and distributed by HUB Pharmaceuticals, LLC. The products were distributed nationwide in the USA.

The Hazard

The recalled strips lack assurance of sterility, posing a risk of infection or other complications if used. These products did not meet current good manufacturing practices, a standard essential for ensuring product safety.

Reported Incidents

There have been no reported injuries or incidents associated with this recall at the time of reporting. Consumers are urged to monitor for any adverse effects.

What to Do

Consumers and healthcare providers should stop using the product immediately. Contact Wizcure Pharmaa or your healthcare provider for guidance on the recall.

Contact Information

For more information, contact Wizcure Pharmaa at email: info@omnilens.in. Additional details are available at the FDA recall website.

Key Facts

  • Recall date: December 31, 2025
  • Reported date: March 4, 2026
  • Quantity recalled: 50,400 boxes
  • Manufacturer: Omni Lens Pvt Ltd, India
  • Distributed by: HUB Pharmaceuticals, LLC

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
All lots
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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